A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv228n97



Internal ID22815625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5680920..5722059hg38UCSC Ensembl
chr5:5681033..5722172hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3841140
hg1941140
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156305, nsv1156304
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv228n97
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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